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M N Patterson

Showing results (11-20 of 29) with videos related to

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Human Genetics|April 1, 1989
Physical mapping of DXS134 close to the DXS52 locusM V Bell, M N Patterson, H R Dorkins, et al.
Archives of Disease in Childhood|December 6, 1997
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UKR M Viner, Y Teoh, D M Williams, et al.
The Quarterly Journal of Medicine|October 1, 1988
Molecular analysis of the fragile X syndromeU Froster-Iskenius, M N Patterson, M V Bell, et al.
Archives of Disease in Childhood|April 1, 1993
Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndromeJ A Batch, H R Davies, B A Evans, et al.
Archives of Disease in Childhood|June 1, 1997
Phenotypic diversity in siblings with partial androgen insensitivity syndromeB A Evans, I A Hughes, C L Bevan, et al.
Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.
Journal of Medical Genetics|September 1, 1993
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalitiesP A Clarkson, H R Davies, D M Williams, et al.
Human Molecular Genetics|February 1, 1996
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndromeC L Bevan, B B Brown, H R Davies, et al.
American Journal of Human Genetics|December 1, 1989
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28M V Bell, J Bloomfield, M McKinley, et al.
Human Molecular Genetics|October 1, 1992
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndromeJ A Batch, D M Williams, H R Davies, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Human Genetics|April 1, 1989
Physical mapping of DXS134 close to the DXS52 locusM V Bell, M N Patterson, H R Dorkins, et al.
Archives of Disease in Childhood|December 6, 1997
Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UKR M Viner, Y Teoh, D M Williams, et al.
The Quarterly Journal of Medicine|October 1, 1988
Molecular analysis of the fragile X syndromeU Froster-Iskenius, M N Patterson, M V Bell, et al.
Archives of Disease in Childhood|April 1, 1993
Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndromeJ A Batch, H R Davies, B A Evans, et al.
Archives of Disease in Childhood|June 1, 1997
Phenotypic diversity in siblings with partial androgen insensitivity syndromeB A Evans, I A Hughes, C L Bevan, et al.
Human Genetics|July 1, 1989
MASA syndrome: further clinical delineation and chromosomal localisationR M Winter, K E Davies, M V Bell, et al.
Journal of Medical Genetics|September 1, 1993
Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalitiesP A Clarkson, H R Davies, D M Williams, et al.
Human Molecular Genetics|February 1, 1996
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndromeC L Bevan, B B Brown, H R Davies, et al.
American Journal of Human Genetics|December 1, 1989
Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28M V Bell, J Bloomfield, M McKinley, et al.
Human Molecular Genetics|October 1, 1992
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndromeJ A Batch, D M Williams, H R Davies, et al.
Pageof 3